98041000119107: Family history of osteogenesis imperfecta (situation)

• SNOMED CT Concept\Situation with explicit context\...
• \Finding with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of development disorder\Family history: Congenital orthopedic anomaly\Family history of osteogenesis imperfecta
• \FH: Musculoskeletal disease\Family history: Congenital orthopedic anomaly\Family history of osteogenesis imperfecta
• \Family history of congenital disease\Family history: Congenital orthopedic anomaly\Family history of osteogenesis imperfecta
• \Family history with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of development disorder\Family history: Congenital orthopedic anomaly\Family history of osteogenesis imperfecta
• \FH: Musculoskeletal disease\Family history: Congenital orthopedic anomaly\Family history of osteogenesis imperfecta
• \Family history of congenital disease\Family history: Congenital orthopedic anomaly\Family history of osteogenesis imperfecta

Status: current, Defined. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3042644015	Family history of osteogenesis imperfecta	en	Synonym	Active	Case insensitive	SNOMED CT core
3042666010	Family history of osteogenesis imperfecta (situation)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

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